Results 11 to 20 of about 1,566 (134)

Synthesis of N-Aryl-3,5-dichloro-4H-1,2,6-thiadiazin-4-imines from 3,4,4,5-Tetrachloro-4H-1,2,6-thiadiazine

open access: yesOrganic Letters, 2015
Condensation of 3,4,4,5-tetrachloro-4H-1,2,6-thiadiazine with a range of anilines gave 22 N-aryl-3,5-dichloro-4H-1,2,6-thiadiazin-4-imines in 43-96% yields. The scope and limitations of this condensation are briefly investigated. Furthermore, mono- and bis-substitution of the C-3 and C-5 chlorines of 3,5-dichloro-N-phenyl-4H-1,2,6-thiadiazin-4-imine by
Kalogirou, Andreas S.   +5 more
core   +6 more sources

Novel Mono-Substituted 4H-1,2,6-Thiadiazines with Antioxidant and Anti-Lipoxygenase Activities. [PDF]

open access: yesInt J Mol Sci
Τhe synthesis of a novel series of mono-substituted 4H-1,2,6-thiadiazine derivatives was reported, aiming at enhancing antioxidant and lipoxygenase inhibitory activities via pharmacophore combination. The compounds were prepared from 3,5-dichloro-4H-1,2,6-thiadiazin-4-one and 2-(3,5-dichloro-4H-1,2,6-thiadiazin-4-ylidene)malononitrile.
Charissopoulos E   +3 more
europepmc   +5 more sources

6-Amino-4-phenylpyrrolo[2,3-c][1,2,6]thiadiazine-5-carbonitrile

open access: yesMolbank
The reaction of 2-(3-chloro-5-phenyl-4H-1,2,6-thiadiazin-4-ylidene)malononitrile with ammonia in anhydrous THF, at ca. 20 °C, for 24 h, gave 6-amino-4-phenylpyrrolo[2,3-c][1,2,6]thiadiazine-5-carbonitrile in 95% yield. The product was characterized by 1H
Andreas S. Kalogirou   +2 more
doaj   +2 more sources

Synthesis of 5′-Chlorospiro(benzo[d][1,3]dioxole-2,4′-[1,2,6]thiadiazin)-3′-amine and 10-Chloro-1,4-dioxa-8-thia-7,9-diazaspiro[4.5]deca-6,9-dien-6-amine

open access: yesMolbank
Reactions of 3′,5′-dichlorospiro(benzo[d][1,3]dioxole-2,4′-[1,2,6]thiadiazine) or 6,10-dichloro-1,4-dioxa-8-thia-7,9-diazaspiro[4.5]deca-6,9-diene with ammonia in MeCN, at ca.
Andreas S. Kalogirou   +1 more
doaj   +2 more sources

Synthesen bicyclischer 1,2,6‐Thiadiazine

open access: yesArchiv der Pharmazie, 1981
Abstractα‐Aminosäureamide aus der Pyrrol‐ Furan‐ und Thiophen‐Reihe werden zu neuen Schwefelheterocyclen umgesetzt. Die Stabilität dieser Verbindungen wird untersucht.
Wolfgang Offermann   +2 more
openaire   +2 more sources

5-Cyano-7-(2-hydroxyphenyl)-4-[(2-hydroxyphenyl)amino]pyrrolo[2,3-c][1,2,6]thiadiazin-6(7H)-iminium Chloride Hydrate

open access: yesMolbank
Reaction of 2-(3,5-dichloro-4H-1,2,6-thiadiazin-4-ylidene)malononitrile with sodium 2-aminophenolate (1.5 equiv.) in anhydrous THF at ca. 0–20 °C afforded the known 4-chlorobenzo[5,6][1,4]oxazino[2,3-c][1,2,6]thiadiazine in 76% yield.
Andreas S. Kalogirou   +2 more
doaj   +2 more sources

Synthesis of Oligomeric 4H‐1,2,6‐Thiadiazines

open access: yesChemistrySelect, Volume 10, Issue 7, February 19, 2025.
The study reports the synthesis of oligomeric amino‐4H‐1,2,6‐thiadiazines that were efficiently obtained in high yields through C─N coupling reactions. Three analogs with terminal phenyl groups, containing up to four thiadiazine units, were prepared, as well as two amino‐substituted bisthiadiazine oligomers.
Andreas S. Kalogirou   +2 more
wiley   +2 more sources

Synthesis of 1,2,6-Thiadiazin 1,1-Dioxide Derivatives as Trypanocidal Agents [PDF]

open access: yesMolecules, 2000
It describes the synthesis of new 1,2,6-Thiadiazin 1,1-dioxide derivatives using condensation of the Knoevenagel type. The products are evaluated in vitro as trypanocidal agents.
H. Cerecetto   +5 more
openaire   +3 more sources

Synthesis of 3-[(2-Ethylhexyl)amino]-5-phenyl-4H-1,2,6-thiadiazin-4-one and 3-[(2-Ethylhexyl)amino]-5-[(4-oxo-5-phenyl-4H-1,2,6-thiadiazin-3-yl)amino]-4H-1,2,6-thiadiazin-4-one

open access: yesMolbank
Suzuki–Miyaura coupling of 3-chloro-5-[(2-ethylhexyl)amino]-4H-1,2,6-thiadiazin-4-one with phenylboronic acid, at ca. 100 °C, gave 3-[(2-ethylhexyl)amino]-5-phenyl-4H-1,2,6-thiadiazin-4-one in 69% yield.
Andreas S. Kalogirou   +1 more
doaj   +2 more sources

The Photochemical Mediated Ring Contraction of 4<i>H</i>-1,2,6-Thiadiazines To Afford 1,2,5-Thiadiazol-3(2<i>H</i>)-one 1-Oxides. [PDF]

open access: yesOrg Lett, 2023
Funding: E.B. and C.G.T. are grateful to Heriot-Watt University and the EPSRC CRITICAT Centre for Doctoral Training (E.B. Ph.D. Studentship: EP/L016419/1, C.G.T Ph.D. Studentship: EP/LO14419/1) for funding and training. C.G.T.
Broumidis E   +12 more
europepmc   +2 more sources

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